Manager, Aesthetics Clinical Development

AbbVie Inc.; Irvine, Lake Forest (CA, CA); On-site; USD 150,000 - 190,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k) plan

Job summary

AbbVie Inc. in Irvine, CA seeks an experienced professional to build scientific reports and present clinical trial data. You will review protocols, contribute to study documents and ensure data integrity across multiple projects.

The role requires leading study development, applying advanced data analysis techniques, coordinating meetings and collaborating with Therapeutic Area teams. Strong communication and proven project leadership are essential.

Qualifications

• Understand complex clinical study principles.
• Advanced ability to analyze clinical study data and generate reports.
• Experience leading scientific projects and teams.
• Experience supporting clinical research, drug development or therapeutic area operations.
• Proven track record of successful projects.
• Attention to detail and strong written/oral communication skills.

Responsibilities

• Prepare scientific reports/presentations for clinical trials using templates and data interpretation.
• Coordinate advisory meeting agendas, activities, slide decks and consulting agreements.
• Ensure compliance with IQS documents, study protocols and directives.
• Lead study development with current electronic document conventions to maintain scientific integrity.
• Receive/complete tasks from function or Therapeutic Area MD within timelines and maximize productivity.
• Participate in process improvement teams and review decisions impacting project timelines.
• Analyze clinical study data, including PK, safety and efficacy reviews using available software.
• Conduct literature/competitive intelligence searches to resolve scientific problems.
• Present key clinical study information to management and therapeutic area teams.
• May lead teams and mentor staff within therapeutic area.

Skills

Scientific data analysis

Clinical study principles

Data presentation

Project coordination

Communication skills

Team leadership

Problem solving

Education

Bachelor's/Master’s degree in Science-related field

PharmD/PhD with 1+ year

Job description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Purpose:

To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.

Responsibilities

• Prepare scientific reports/presentations related to clinical trials using available software and templates and; review/contribute to clinical protocols, by utilizing expertise, to assist in interpretation of data.
• Coordinate advisory meeting agendas, activities and slide decks and consulting agreements.
• Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.
• Lead the study development by applying most current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes.
• Responsible for receiving and completing tasks and assignments from function, Therapeutic Area MD or Scientific Staff within timeline with minimal supervision and; maximizing individual, function/therapeutic area and team productivity.
• Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
• Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews and ensure the scientific integrity of all processes.
• Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
• Provide/present key clinical study information to function/therapeutic area and management.
• May lead teams within therapeutic area and supervise exempt and/or non-exempt direct reports and mentor function/-therapeutic area personnel.

Qualifications

• Bachelors/Master’s degree, in Science related to Field with 11+ years’ experience in the pharmaceutical industry or Pharm-D/PhD with 1+years.
• Ability to understand more complex clinical study principles.
• Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters and manuscripts.
• Experience in team, drug development, and scientific project leadership or related.
• Experience supporting clinical research, drug development and/or function/therapeutic area operations.
• Must have a proven record of successful projects.
• Experience in multi-faceted, broad-based multiple functions/therapeutic areas or clinical functions with in depth knowledge of clinical study issues.
• Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
• Ability to produce work of the highest quality by paying attention to detail.
• Must possess good oral and written communication skills.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html